Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP244163.RAUwIR6bW_wA_YysJBUr88LpShSvEjBEMxfX-MBVEWgzk130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP244163.RAUwIR6bW_wA_YysJBUr88LpShSvEjBEMxfX-MBVEWgzk130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP244163.RAUwIR6bW_wA_YysJBUr88LpShSvEjBEMxfX-MBVEWgzk130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP244163.RAUwIR6bW_wA_YysJBUr88LpShSvEjBEMxfX-MBVEWgzk130_provenance.
- befree-20150227 importedOn "2015-02-27" NP244163.RAUwIR6bW_wA_YysJBUr88LpShSvEjBEMxfX-MBVEWgzk130_provenance.
- NP244163.RAUwIR6bW_wA_YysJBUr88LpShSvEjBEMxfX-MBVEWgzk130_assertion wasGeneratedBy ECO_0000203 NP244163.RAUwIR6bW_wA_YysJBUr88LpShSvEjBEMxfX-MBVEWgzk130_provenance.
- NP244163.RAUwIR6bW_wA_YysJBUr88LpShSvEjBEMxfX-MBVEWgzk130_assertion wasDerivedFrom befree-20150227 NP244163.RAUwIR6bW_wA_YysJBUr88LpShSvEjBEMxfX-MBVEWgzk130_provenance.
- NP244163.RAUwIR6bW_wA_YysJBUr88LpShSvEjBEMxfX-MBVEWgzk130_assertion SIO_000772 10984082 NP244163.RAUwIR6bW_wA_YysJBUr88LpShSvEjBEMxfX-MBVEWgzk130_provenance.
- NP244163.RAUwIR6bW_wA_YysJBUr88LpShSvEjBEMxfX-MBVEWgzk130_assertion evidence source_evidence_literature NP244163.RAUwIR6bW_wA_YysJBUr88LpShSvEjBEMxfX-MBVEWgzk130_provenance.
- NP244163.RAUwIR6bW_wA_YysJBUr88LpShSvEjBEMxfX-MBVEWgzk130_assertion description "[Familial defective apolipoprotein B-100 (FDB) is a genetic disorder caused by a substitution of glutamine for arginine at residue 3500 of the apolipoprotein B-100 molecule.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP244163.RAUwIR6bW_wA_YysJBUr88LpShSvEjBEMxfX-MBVEWgzk130_provenance.